Evidence map›Paper›PMID 40603781›Full record

ReviewAdvances in experimental medicine and biology2025

Cellular Iron Homeostasis.

Caroline C Philpott, Esther G Meyron-Holtz

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances in experimental medicine and biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Caroline C PhilpottGenetics and Metabolism Section, Liver Diseases Branch, NIDDK, NIH, Bethesda, MD, USA. carolinep@intra.niddk.nih.gov.
Esther G Meyron-HoltzLaboratory of Molecular Nutrition, Faculty of Biotechnology and Food Engineering, Technion, Haifa, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Iron is an essential nutrient for all eukaryotic cells, yet it is potentially toxic. Cells have elegant systems coordinating the uptake, use, storage, and export of this metal while also responding to extracellular cues for regulating uptake and efflux. Here we describe the basic systems that operate in all cells with the goal of maintaining iron homeostasis in a highly dynamic system. In mammalian tissues and organs, multiple cell types are highly specialized in their iron management with the goal of maintaining cellular homeostasis subordinate to achieving a more specific function, e.g., dietary iron absorption in the intestinal epithelium, hemoglobin synthesis in the erythron, and iron recycling in splenic macrophages. The alterations in cellular iron balance that allow for these specializations will be briefly discussed.

Indexed as

HomeostasisIronAnimalsHemoglobinsHumansIntestinal MucosaMacrophagesHemoglobinsIronCellular iron traffickingFerritinHemeIron regulatory proteinsIron-sulfur clusters

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.